Tseng C P, Ely B D, Li Y, Pong R C, Hsieh J T
Department of Urology, University of Texas Southwestern Medical Center, Dallas 75235-9110, USA.
Endocrinology. 1998 Aug;139(8):3542-53. doi: 10.1210/endo.139.8.6159.
Androgen is a mitogen as well as a morphogen for prostatic epithelium. However, the detailed mechanisms of these distinct androgenic actions have not yet been delineated. Therefore, we employed differential display PCR to unveil any potential genes that may be involved in these processes. In this study, we report the isolation and characterization of two alternative splicing forms (p82 and p59) of C9 complementary DNA, the rat homolog of the human deletion of ovarian carcinoma 2 (DOC-2) gene and mouse p96 phosphoprotein, from rat ventral prostate (VP). We found that C9 was up-regulated in rat VP after castration, suggesting that C9 may be regulated by androgen receptor directly or indirectly during prostate degeneration. A similar regulatory pattern was also observed in both the seminal vesicle and dorsolateral prostate, but not in the coagulating gland or other androgen-independent organs. Immunohistochemical analysis of rat VP demonstrated that C9 is detected in the basal epithelia and surrounding stromal cells after prolonged castration. Ribonuclease protection assay and Western blot analysis revealed that p59 is the predominant C9 isoform in rat VP. To unveil the function of C9 in cell growth, we transfected p59 complementary DNA into the C4-2 cells, a derivative of the LNCaP prostatic carcinoma cell line. The p59 stable transfectants exhibited a slower growth rate and an increase in the cell fraction in the G1 phase under our experimental conditions. These data indicate that C9-p59 has growth inhibitory activity for prostatic epithelial cells. Taken together, our results suggest that C9 is up-regulated during prostate degeneration process and may play an active role in the proliferation and differentiation of prostatic epithelium.
雄激素是前列腺上皮细胞的促分裂原和形态发生素。然而,这些不同雄激素作用的详细机制尚未阐明。因此,我们采用差异显示PCR技术来揭示可能参与这些过程的任何潜在基因。在本研究中,我们报道了从大鼠腹侧前列腺(VP)中分离和鉴定出C9互补DNA的两种可变剪接形式(p82和p59),它们分别是人类卵巢癌缺失2(DOC-2)基因和小鼠p96磷蛋白的大鼠同源物。我们发现,去势后大鼠VP中C9表达上调,这表明在前列腺退化过程中C9可能直接或间接受到雄激素受体的调控。在精囊和背外侧前列腺中也观察到了类似的调控模式,但在凝固腺或其他雄激素非依赖性器官中未观察到。对大鼠VP的免疫组织化学分析表明,长期去势后,在基底上皮细胞和周围基质细胞中可检测到C9。核糖核酸酶保护试验和蛋白质印迹分析显示,p59是大鼠VP中主要的C9同工型。为了揭示C9在细胞生长中的功能,我们将p59互补DNA转染到C4-2细胞中,C4-2细胞是LNCaP前列腺癌细胞系的衍生物。在我们的实验条件下,p59稳定转染子表现出较慢的生长速度和G1期细胞比例增加。这些数据表明,C9-p59对前列腺上皮细胞具有生长抑制活性。综上所述,我们的结果表明,C9在前列腺退化过程中表达上调,可能在前列腺上皮细胞的增殖和分化中发挥积极作用。